Substrate Having a Burnable Coating Mask

ABSTRACT

A substrate having a burnable coating mask includes: a substrate having a first section and a second section; a mask coating layer over the first section of the substrate; and a functional coating layer over at least a portion of the mask coating layer and over the second section of the substrate. A method of segmenting a substrate having a layer thereover, a method of preparing a segmented substrate having a layer thereover, a segmented substrate, and a transparency are also disclosed.

CROSS REFERENCE TO RELATED APPLICATIONS

This application claims priority to and is a continuation of U.S. Pat.Application No. 16/913,305, filed on Jun. 26, 2020, which claimspriority to U.S. Provisional Pat. Application No. 62/868,324, filed onJun. 28, 2019 and to U.S. Provisional Pat. Application No. 63/018,596,filed on May 1, 2020, each of which is incorporated herein by referencein its entirety.

BACKGROUND OF THE INVENTION Field of the Invention

The present invention is directed to a substrate having a burnablecoating mask, a method of segmenting a substrate having a layerthereover, a method of preparing a segmented substrate having a layerthereover, a segmented substrate, and a transparency.

Description of Related Art

For certain applications, a substrate may be desired that has afunctional coating over certain sections of the substrate and nofunctional coating over other sections of the substrate. As one example,some automakers utilize infrared cameras or rain detectors whose sensorsare interfered with by the presence of the functional coating overcertain sections of the substrate through which the sensor transmitsinfrared (or other) radiation.

One procedure to manufacture such a substrate is to use laser deletionto remove the functional coating from the relevant sections of thesubstrate. However, some customers have rejected substrates manufacturedusing laser deletion because laser deletion technology incompletelyremoves the functional coating in certain cases.

Therefore, it is desired to produce a substrate with a functionalcoating over certain sections of the substrate and no functional coatingover other sections of the substrate without the use of laser deletion.

SUMMARY OF THE INVENTION

The present invention is directed to a substrate having a burnablecoating mask, including: a substrate having first surface and a secondsurface opposite the first surface. The first surface has a firstsection and a second section adjacent the first section. A mask coatinglayer is positioned over the first section of the first surface. Themask coating layer is not positioned over the second section of thefirst surface. A functional coating layer is positioned over at least aportion of the mask coating layer and over the second section of thesubstrate. When the coated substrate is heated, the burnable coatingmask, and a portion of the functional coating layer over the burnablecoating mask is removed leaving an area on the substrate that does nothave a functional coating layer.

The present invention is also directed to a method of segmenting asubstrate. A substrate having a burnable coating mask is provided. Thesubstrate includes a first surface and a second surface opposite thefirst surface. The first surface has a first section and a secondsection adjacent the first section. A mask coating layer is positionedover the first section. The mask coating layer is not positioned overthe second section of the first surface. A functional coating layer ispositioned over at least a portion of the mask coating layer and overthe second section of the substrate. The coated substrate is heated sothat the mask coating layer is removed from the first section. A portionof the functional coating positioned over the mask coating layer is alsoremoved from the first section. The portion of the functional coatingpositioned over the second section remains substantially intake on thesubstrate.

The present invention is also directed to a method of preparing asegmented substrate. A substrate having first surface and a secondsurface opposite the first surface is provided. The first surface has afirst section and a second section adjacent the first section. Amaterial is applied over the first section of the first surface to forma mask coating layer. The mask coating layer is not positioned over thesecond section of the first surface. A functional coating layer isapplied over at least a portion of the mask coating layer and over thesecond section of the first surface to form a functional coating layer.

The present invention is also directed to a method of preparing anautomotive transparency, including: providing a first ply having a No. 1surface and an No. 2 surface opposite the No. 1 surface; providing asecond ply having a No. 3 surface and a No. 4 surface opposite the No. 3surface; the No. 1 surface, No. 2 surface, the No. 3 surface or No. 4surface having a first section and a second section adjacent the firstsection; a mask coating layer over the first section wherein the maskcoating layer is not present over the second section; and a functionalcoating layer over at least a portion of the mask coating layer and overthe second section; heating the first ply and the second ply eithersimultaneously or separately and removing the mask coating layer and aportion of the functional coating that is positioned over the maskcoating layer to form the automotive transparency.

BRIEF DESCRIPTION OF THE DRAWINGS

FIGS. 1A-3A show cross-sectional views of substrates having a burnablecoating mask according to some non-limiting embodiments;

FIGS. 1B-3B show cross-sectional views of segmented substrates preparedusing a burnable coating mask according to some non-limitingembodiments;

FIG. 4 shows a plan view of a segmented substrate according to somenon-limiting embodiments;

FIG. 5 shows a cross-sectional view of a transparency according to somenon-limiting embodiments; and

FIG. 6 shows a micrograph of a coated substrate comprising a maskcoating layer after heating.

DESCRIPTION OF THE INVENTION

For purposes of the description hereinafter, the terms “end”, “upper”,“lower”, “right”, “left”, “vertical”, “horizontal”, “top”, “bottom”,“lateral”, “longitudinal”, and derivatives thereof shall relate to theinvention as it is oriented in the drawing figures. However, it is to beunderstood that the invention may assume various alternative variationsand step sequences, except where expressly specified to the contrary. Itis also to be understood that the specific devices and processesillustrated in the attached drawings, and described in the followingspecification, are simply exemplary embodiments or aspects of theinvention. Hence, specific dimensions and other physical characteristicsrelated to the embodiments or aspects disclosed herein are not to beconsidered as limiting.

For purposes of the following detailed description, it is to beunderstood that the invention may assume various alternative variationsand step sequences, except where expressly specified to the contrary.Accordingly, unless indicated to the contrary, the numerical parametersset forth in the following specification and attached claims areapproximations that may vary depending upon the desired properties to beobtained by the present invention. At the very least, and not as anattempt to limit the application of the doctrine of equivalents to thescope of the claims, each numerical parameter should at least beconstrued in light of the number of reported significant digits and byapplying ordinary rounding techniques.

It should be understood that any numerical range recited herein isintended to include all sub-ranges subsumed therein. For example, arange of “1 to 10” is intended to include all sub-ranges between (andincluding) the recited minimum value of 1 and the recited maximum valueof 10, that is, having a minimum value equal to or greater than 1 and amaximum value of equal to or less than 10.

With respect to layers of material described herein, the term “over”means farther from the substrate on which the material is positioned.For example, a second layer positioned “over” a first layer means thatthe second layer is positioned farther from the substrate than is thefirst layer. The second layer may be in direct contact with the firstlayer. Alternatively, one or more other layers may be positioned betweenthe first layer and the second layer.

The terms “polymer” or “polymeric” include oligomers, homopolymers,copolymers, and terpolymers, e.g., polymers formed from two or moretypes of monomers or polymers.

As used herein, the transitional term “comprising” (and other comparableterms, e.g., “containing” and “including”) is “open-ended” and open tothe inclusion of unspecified matter. Although described in terms of“comprising”, the terms “consisting essentially of” and “consisting of”are also within the scope of this disclosure.

It will be appreciated that components in FIGS. 1A-5 having the samelast two digits in their element number correspond to components fromthe other FIGS. in the application and include the same characteristicsof the corresponding components, except where expressly described. Forexample, components 102, 202, 302, and the like all refer to thesubstrate described hereinafter since all of these element numbers havethe same last two digits (02).

Referring to FIG. 1A, a substrate 100 having a burnable coating mask isshown according to some non-limiting embodiments. The substrate 100having a burnable coating mask may include a substrate 102 having afirst section 104 and a second section 106 on a surface thereof. Thesubstrate 102 may be made of any suitable material. The substrate 102may be transparent or translucent to visible light. By “transparent” ismeant having visible light transmission of greater than 0% up to 100%.By “translucent” is meant allowing electromagnetic energy (e.g., visiblelight) to pass through but diffusing this energy such that objects onthe side opposite the viewer are not clearly visible. Examples of suchmaterials include, but are not limited to, plastic substrates (such asacrylic polymers, such as polyacrylates; polyalkylmethacrylates, such aspolymethylmethacrylates, polyethylmethacrylates,polypropylmethacrylates, and the like; polyurethanes; polycarbonates;polyalkylterephthalates, such as polyethyleneterephthalate (PET),polypropyleneterephthalates, polybutyleneterephthalates, and the like;polysiloxane-containing polymers; or copolymers of any monomers forpreparing these, or any mixtures thereof); ceramic substrates; glasssubstrates; or mixtures or combinations of any of the above. Forexample, the substrate 102 can include conventional soda-lime-silicateglass, borosilicate glass, or leaded glass. The glass may be uncoatedglass. The glass can be clear glass. By “clear glass” is meantnon-tinted or non-colored glass. Alternatively, the glass can be tintedor otherwise colored glass. The glass can be of any type, such asconventional float glass, and can be of any composition having anyoptical properties, e.g., any value of visible transmission, ultraviolettransmission, infrared transmission, and/or total solar energytransmission. By “float glass” is meant glass formed by a conventionalfloat process in which molten glass is deposited onto a molten metalbath and controllably cooled to form a float glass ribbon. Examples offloat glass processes are disclosed in U.S. Pat. Nos. 4,466,562 and4,671,155.

The substrate 102 can each be, for example, clear float glass or can betinted or colored glass. Although not limiting, examples of glasssuitable for the substrate 102 are described in U.S. Pat. Nos.4,746,347; 4,792,536; 5,030,593; 5,030,594; 5,240,886; 5,385,872; and5,393,593. The substrate 102 can be of any desired dimensions, e.g.,length, width, shape, or thickness. In one exemplary substrate used inan automotive transparency, the substrate 102 can be 1 mm to 10 mmthick, such as 1 mm to 8 mm thick, such as 2 mm to 8 mm, such as 3 mm to7 mm, such as 5 mm to 7 mm, such as 6 mm thick. Non-limiting examples ofglass that can be used for the practice of the disclosure includes clearglass, Starphire®, Solargreen®, Solextra®, GL-20®, GL-35™, Solarbronze®,Solargray® glass, Pacifica® glass, SolarBlue® glass, and Optiblue®glass, all commercially available from PPG Industries Inc. ofPittsburgh, Pennsylvania.

With continued reference to FIG. 1A, the substrate 100 having a burnablecoating mask may include a material that may be applied over the firstsection 104 of the substrate 102 to form a mask coating layer 108, butnot over the second section 106 of the substrate. The mask coating layer108 may be selectively positioned over certain section(s) of thesubstrate 102 (e.g., the first section 104), while avoiding beingpositioned over other section(s) of the substrate 102 (e.g., the secondsection 106). The mask coating layer 108 may be formed directly over thesubstrate 102 (so as to be in direct contact therewith), or the maskcoating layer 108 may be formed indirectly over the substrate 102(having at least one intervening coating layer between the substrate 102and the mask coating layer 108). Preferably the masking coating layer108 is formed directly onto the substrate 100. The mask coating layer108 may be applied using any suitable application method including, butnot limited to inkjet printing, silk screen printing, stamping, and thelike. The method may further include preparing the material via anemulsion, where the material is dispersed in water or an aqueous medium.As used herein, an “aqueous medium” is a liquid mixture comprisinggreater than 50% water. It is appreciated that greater than 50% water iswith respect to the total liquid content, such that any solids presentare not taken into consideration. The mask coating layer 108 may have athickness ranging from 10 nm to 2000 µm, such as 10 nm to 1,000 µm, 10nm to 500 µm, 0.5 µm to 100 µm, 0.5 µm to 10 µm, 10 µm to 30 µm, or 50µm to 100 µm.

The mask coating layer 108 may include a material including wax, anorganic oil (e.g., tung oil), a polyolefin, a (meth)acrylate (e.g., apoly(meth)acrylate) (as will be understood herein, (meth)acrylate refersto both acrylate and methacrylate), a polyester, an alkene, apolyethylene, a polypropylene, an emulsion thereof, or some combinationthereof. The mask coating layer 108 may comprise polylactic acid (PLA),polyethylene carbonate (PEC), polypropylene carbonate (PPC),polycaprolactone, polyoxymethylene, polyethylene, polypropylene, or somecombination thereof. The wax may include stearic acid, paraffin,carnauba, microcrystalline wax, polyethylene wax, or some combinationthereof. Examples of wax emulsions include those available fromMichelman, Inc. (Cincinnati, OH) (e.g., MGRD 1350, ML160, ME62330,Aqua240 PH90602L, ME48040M2) or BYK-Chemie GmbH (Wesel, Germany) (e.g.,AQUACER 526, AQUACER541, AQUACER 1031, AQUACER 8500). The wax emulsionmay be a paraffin/polyethylene emulsion, an anionic polyamide emulsion,an anionic carnauba emulsion, an amine dispersed carnauba emulsion, anethylene acrylic acid emulsion, a non-ionic microcrystalline emulsion,or some combination thereof. In some non-limiting examples, the maskcoating layer 108 may include an alkane, an ester, or a carboxylic acidand have at least 40 wt.% carbon, based on the total weight of the maskcoating layer 108, such as at least 50 wt.%, at least 60 wt.%, at least70 wt.%, at least 80 wt.%, or at least 90 wt.%. The material may bemixed with a solvent. For example, the material may include a mixture ofPLA and methyl acetate.

Alternatively, or in addition to any of the aforementioned materials ofthe mask coating layer 108 may include a polyurethane material, anepoxide material, a polyurea material, or a combination thereof. As usedherein, a “polyurethane material” is a material that forms at least aportion of the mask coating layer 108 and which comprises urethanelinkages and/or is made from components comprising a polyurethane.Examples of polyurethanes that may be used include aqueouspolyurethanes, polyurethanes formed from a two component system,emulsions thereof, and combinations thereof. The polyurethanes maycomprise additional functional groups including ester linkages, etherlinkages, and hydrophilic groups such as hydroxyl groups, carboxylgroups, carbonyl groups, amino groups, thiols, and the like. Hydrophilicfunctional groups may be incorporated into the polyurethane to aid inthe formation of an emulsion. The polyurethanes can be obtained byreacting one or more hydroxyl functional compounds with one or moreisocyanate functional compounds. The hydroxyl functional compounds caninclude diols and/or polyols having 3 or more hydroxyl functionalgroups. The isocyanate functional compounds can include compounds having2 or more isocyanate functional groups, such as 3 or more isocyanatefunctional groups. The isocyanate functional compounds can compriseunblocked isocyanates, blocked isocyanates, partially blockedisocyanates, or a combination thereof.

As indicated, the mask coating layer 108 may include an epoxidematerial. As used herein, an “epoxide material” is a material thatcomprises an epoxide or that is obtained from components comprising anepoxide. Examples of epoxides include epoxy functional polymericmaterials, which is also known as a polyepoxide and which comprises twoor more epoxy functional groups. The epoxides may be an emulsion. Theepoxide can comprise one or more additional functional groups (e.g.carboxylic acid and/or hydroxyl functional groups) and be reactive withitself as a self-crosslinkable compound to form the reaction product.Alternatively, the epoxide can be reacted with a second compound such asa carboxylic acid and/or hydroxyl functional compound to form thereaction product. The epoxide may also comprise epoxy functional groupswhen there are excess epoxy functional groups in the reactants.Alternatively, the epoxy functional groups may all react during thereaction to form the epoxide layer such that no epoxy functional groupsare present in the mask coating layer 108.

As indicated, the mask coating layer 108 may include a polyureamaterial. As used herein, a “polyurea material” is a material thatcomprises urea linkages and/or is formed from components comprising apolyurea.

The mask coating layer 108 may include both a polyurethane material andan epoxide material. If both a polyurethane material and an epoxidematerial are present, the polyurethane material and epoxide material maybe formed together such that the mask coating layer 108 comprises onelayer comprising both a polyurethane and an epoxide. Alternatively, ifboth a polyurethane material and an epoxide material are present, thepolyurethane material and epoxide material may be formed as separatelayers. For example, the polyurethane material may be formed over thesubstrate and the epoxide material may be formed over the polyurethanematerial as separate layers. As a further example, the epoxide materialmay be formed over the substrate and the polyurethane material may beformed over the epoxide material as separate layers.

As used herein, the terms “one-component” or “1K” refer to a coatingcomposition wherein all of the coating components are combined andstored in a single container. As used herein, the terms “two-component”or “2K” refer to a coating composition wherein the components are storedseparately and, when mixed with one another, react to crosslink to forma crosslinked material.

The material applied to form the mask coating layer 108 may be athermoplastic or thermoset. As used herein, a “thermoplastic” is amaterial that softens when heated and has a defined melting point. Thematerial applied to form the mask coating layer 108 may be a thermosetof any of the previously mentioned materials of the mask coating layer108. As used herein, a “thermoset” is any crosslinked material that doesnot have a defined melting point, and instead burns or decomposes whenheated. The material applied to form the mask coating layer 108 may havea low degree of cross-linking such that the material has a definedmelting temperature. The material applied to form the mask coating layer108 may have a high degree of cross-linking such that the material doesnot have a defined melting temperature. A high degree of cross-linkingcan be achieved, for example, via solvent based formulations or by theaddition of a crosslinker to an aqueous formulation.

The mask coating layer 108 may include a material that when included ina composition and applied to a substrate and solidified to form a layer,the layer exhibits a water contact angle (WCA) (upon contact with water)of at least 60°, such as at least 70°, or at least 80°. The mask coatinglayer 108 may include a hydrophobic material. A hydrophobic material isdefined herein as a material that when included in a composition andapplied to a substrate and solidified to form a layer, the layerexhibits a WCA (upon contact with water) of at least 90°, such as atleast 100°, at least 110°, at least 120°, at least 130°, at least 140°,or at least 150°.

The mask coating layer 108 may include a material having a melting pointof at least 60° C., such as at least 70° C. or at least 80° C. The maskcoating layer 108 may have a melting point of from 60° C.-350° C. Themask coating layer 108 may include a material that, when solidified, isimpermeable to water and other standard processing liquids, such ascooling agents, cutting oils, and the like. The mask coating layer 108may provide increased corrosion protection to the substrate 102 comparedto the same substrate not including the mask coating layer 108positioned thereover.

In some non-limiting examples, the material applied to form the maskcoating layer 108 may include an emulsion comprising a hydrophobicmaterial, water, and a surfactant, and the surfactant may be a non-ionicsurfactant or an ionic surfactant (e.g., a cationic or an anionicsurfactant). The material applied to form the mask coating layer 108 mayinclude a material comprising a hydrophobic material dissolved in asolvent. The material applied to form the mask coating layer may includea UV curable or heat curable material that, when applied to the surfaceof the substrate and exposed to a UV source or heat source, results incrosslinking of the applied material on the substrate. The materialapplied to form the mask coating layer may include a two component (2 K)resin that includes separate components that, when mixed with oneanother, react to crosslink the material upon application of thematerial to the surface of the substrate.

In some non-limiting examples, the material is heated until itstemperature is at least the glass transition temperature (“Tg”) of thematerial, and the material is applied at the temperature that is atleast the Tg of the material. In other non-limiting examples thematerial is applied at a temperature below the Tg of the material andsubsequently heated to a temperature suitable for the material tosoften, such as above the Tg of the material. A non-limiting exampleincludes Carnauba wax, such as ML160, available from Michelman, Inc.(Cincinnati, OH), which may require a heat treatment to a temperatureabove its Tg of 63° C., such as at least 70° C., at least 80° C., or atleast 90° C. The material may also require a curing step at atemperature for a period of time. For example, the material may be curedat room temperature (i.e., in the range of 20-27° C., such as 25° C.)for a period of time of up to 72 hours, or up to 48 hours, or up to 36hours, or up to 24 hours. The material may also be cured at an elevatedtemperature, such as in the range of 90-180° C., or 100-170° C., or110-150° C., or 120-130° C. (such as 121° C.), for a period of time ofup to 2 hours, such as 1 hour, such as 30 minutes, such as 15 minutes.

The mask coating layer 108 may comprise optional additional components.Non-limiting examples of additional components include plasticizers,crosslinkers, viscosity modifiers, corrosion inhibitors, infrared (IR)absorbers, adhesion modifiers, UV absorbers, pigments, surfactants, andhydrophobic agents. An example of suitable plasticizers for use in thecomposition of the mask coating layer 108 include oils such as cottonseed oil, epoxidized soybean oil, and canola oil, waxes such as carnaubawax, paraffin, and microcrystalline wax, polyethylene glycol, andpolypropylene glycol. Plasticizers are included in the mask coatinglayer 108 composition to aid in the removal of the mask coating layer108 via abrasion wheels, especially when the mask coating layer 108 is athermoset resin system. A plasticizer may be included in the maskcoating layer 108 in an amount in the range of 1 to 50 wt%, or 4 to 40wt%, or 10 to 30 wt%, based on the total solid components of the maskcoating layer 108.

Examples of suitable viscosity modifiers include RHEOBYK-425, RHEOBYK-T1000VF, RHEOBYK-L 1400 VF, and RHEOBYK-H 3300 VF commercially availablefrom BYK and H1335 and HY124 commercially available from Spectrum. Aviscosity modifier may be included in the mask coating layer 108 in anamount in the range of 0.05 to 20 wt%, or 0.1 to 15 wt%, or 0.1 to 10wt%, based on the total components of the coating mask layer 108.

Examples of suitable hydrophobic agents include waxes, oils, and fattyacids. A hydrophobic agent may be included in the mask coating layer 108in an amount in the range of 0.5 to 70 wt%, or 1 to 65 wt%, or 1 to 60wt%, based on the total solid components of the mask coating layer 108.

Examples of suitable crosslinkers for use in the mask coating layer 108composition include compounds containing an aziridine group. Anon-limiting example of a compound that includes an aziridine group thatmay be used in the mask coating layer 108 is trimethylolpropanetris(2-methyl-1-aziridinepropionate). A crosslinker may be included inthe mask coating layer 108 in an amount in the range of 0.05 to 30 wt%,or 0.1 to 20 wt%, or 0.1 to 10 wt%, based on the total solid componentsof the mask coating layer 108. Crosslinkers are included in the maskcoating layer 108 composition in order to crosslink the composition,such as to create a thermoset resin system.

The mask coating layer 108 may comprise inorganic compounds, such astalc, silica, metallic catalysts, inorganic pigments, and the like.Alternatively, one or more of the coating layers (e.g. one or all of thecoating layers) may be free of any of the previously describedadditional components, such as being free of inorganic compounds such astalc, silica, metallic catalysts, inorganic pigments, and the like.

Additional additives, such as crosslinkers, may be added duringpreparation of the material that forms the mask coating layer 108.Alternatively, the additional additives may be added right before thematerial is applied to form the mask coating layer 108.

With continued reference to FIG. 1A, substrate 100 having a burnablecoating mask may include a functional coating material applied over atleast a portion of the mask coating layer 108 and over the secondsection 106 of the substrate 102 to form a coating layer 110. Thecoating layer 110 may have a functional coating layer. The coating layer110 may have a protective layer over the functional coating layer. Thefunctional coating layer may have a thickness of less than 1 µm.

As used herein, the term “functional coating layer” refers to a coatingwhich imparts a functional benefit to the surface beyond decoration ofthe surface. Non-limiting examples include coatings that impart anoptical property, structural property, electrical property, hygienicproperty, thermal property, and/or physio-chemical property to thesurface. Non-limiting examples of functional coatings include at leastone of a low-e (low-emissivity) coating, a hydrophilic coating, ahydrophobic coating, an oleophilic coating, a low friction coating, ananti-microbial coating, an anti-fingerprint coating, an anti-fogcoating, a self-cleaning coating, an easy-clean coating, a transparentconductive coating, and combinations thereof. The functional coatinglayer may include a solar control coating. As used herein, the term“solar control coating” refers to a coating comprised of one or morelayers or films that affect the solar properties of the coated article,such as, but not limited to, the amount of solar radiation, for example,visible, infrared, or ultraviolet radiation, reflected from, absorbedby, or passing through the coated article; shading coefficient;emissivity, etc.; the solar control coating can block, absorb, or filterselected portions of the solar spectrum, such as, but not limited to,the IR, UV, and/or visible spectrums.

The functional coating layer may be a single-layer or multi-layercoating. The functional coating layer may be a multi-layer solar controlcoating, such as is described in US 2017/0341977.

The functional coating layer may include any temperable coating layer,for example, those disclosed in British Patent No. GB 2,302,102; U.S.Pat. No. 4,504,109; U.S. Pat. No. 4,952,423; U.S. Pat. No. 5,028,759;U.S. Pat. No. 5,059,295; U.S. Pat. No. 5,653,903; U.S. Pat. No.7,749,621; U.S. Pat. No. 8,865,325; U.S. Published Pat. Application No.2014/0272453. The functional coating layer may include coatingsavailable under the tradename Solarban® or Sungate®, commerciallyavailable from Vitro Architectural Glass (Cheswick, PA).

The functional coating layer may comprise a metallic layer comprising ametallic material, such as gold, copper, aluminum, palladium, or acombination thereof. The functional coating layer may be applied to thesubstrate using magnetron sputtering vapor deposition (“MSVD”), such asa MSVD coated glass. Non-limiting examples of suitable functionalcoatings and coated substrates are disclosed in US 2017/0341977; US2018/0118614; US 2019/0204480; US 7,335,421; US 8,865,325; US 9,932,267;and US 10,479,724; all of which are incorporated herein by reference intheir entirety.

A protective layer may be applied over the functional coating layer. Theprotective layer can help protect the underlying coating layers, such asfunctional coating layer and any of its component films and layers, frommechanical and/or chemical attack. The protective layer may be comprisedof Si₃N₄, SiAlN, SiAlON, titania, alumina, silica, zirconia, tin oxide,a mixture thereof, and/or an alloy thereof, and which may provideincreased durability to the functional coating layer. For example, theprotective layer can be SiAlN, Si₃N₄, TiAlO or TiO₂. The protectivelayer can have a thickness in the range of 10 Å to 800 Å, such as 100 Åto 800 Å, such as 100 Å to 400 Å, such as 350 Å to 400 Å; or a thicknessrange of 100 Å to 400 Å, such as 200 Å to 300 Å, such as 270 Å to 330 Å,such as 10 Å to 80 Å, such as 45 Å to 55 Å. The protective layer may bethe uppermost layer of the substrate.

Referring to FIG. 2A, a substrate 200 having a burnable coating mask isshown according to some non-limiting embodiments. The substrate 200having a burnable coating mask may have the same characteristics as thesubstrate 100 having a burnable coating mask as described in FIG. 1Aexcept as follows. The substrate 200 having a burnable coating mask mayfurther include a temporary protective material applied over at least aportion of the coating layer 210 to form a temporary protective layer212. The temporary protective layer 212 may be positioned over theentire substrate 202 or selectively positioned over certain sections ofthe substrate 202. The temporary protective layer 212 may be anoutermost layer over the substrate 202.

The material used to form the temporary protective layer 212 may includeany of the previously-described materials used to form the mask coatinglayer 208. The temporary protective layer 212 may be formed from thesame or different of those materials compared to the mask coating layer208.

Referring to FIG. 3A, a substrate 300 having a burnable coating mask isshown according to some non-limiting embodiments. The substrate 300having a burnable coating mask may have the same characteristics as thesubstrate 100 having a burnable coating mask as described in FIG. 1Aexcept as follows. As shown in FIG. 1A, the coating layer 110 may have anon-uniform thickness, such that the coating layer 110 has a firstthickness over the second section 106 and has a second thickness overthe first section 104. The first thickness may be thicker than thesecond thickness. The first thickness and the second thickness may besuch that the surface of the coating layer 110 is substantially the samedistance from the substrate 102 across the entire coating layer 110. Thesubstrate 300 having a burnable coating mask in FIG. 3A is differentthan the substrate 100 having a burnable coating mask in FIG. 1A, inthat the substrate 300 having a burnable coating mask in FIG. 3A has acoating layer 310 having a substantially uniform thickness (e.g., within5% of the average thickness across the entire coating layer 310). Inthis way, the surface of the coating layer 310 may be a differentdistance from the substrate 302 in certain sections of the coating layer310. For example, as shown in FIG. 3A, the surface of the coating layer310 over the first section 304 may be farther from the substrate 302than the surface of the coating layer 310 over the second section 306 bythe thickness of the mask coating layer 308.

Referring to FIGS. 1B-3B, segmented substrates 101, 201, 301 preparedusing a burnable coating mask are shown. The segmented substrates 101,201, 301 from FIGS. 1B-3B correspond to the substrates 100, 200, 300having a burnable coating mask from FIGS. 1A-3A, respectively, after thesubstrates 100, 200, 300 having a burnable coating mask have undergone aheat treatment process to form the segmented substrates 101, 201, 301.The heat treatment process may remove the mask coating layer and/or thetemporary protective layer. The section of the coating layer positionedover the mask coating layer may be removed during the heat treatmentprocess as a result of the mask coating layer thereunder being removed.Upon the mask coating layer being removed by the heat treatment process,the first section of the substrate may be exposed.

The material used to form the mask coating layer and/or the temporaryprotective layer may be “burnable” so as to be removable by the heattreatment process. As used in this disclosure, the term “burnable”refers to a material that will burn, evaporate, or otherwise thermallydecompose from the substrate, interacting with the substrate orotherwise substantially damaging (as defined hereinafter) the aestheticsor performance of the substrate (including any coating thereover).Burnable materials may burn, evaporate or otherwise thermally decomposeat least when the temperature of the substrate is from 500° C. to 1000°C. It is anticipated that the burnable material will burn, evaporate, orotherwise thermally decompose before the substrate reaches a temperatureof 1000° C., such as a temperature of 900° C., 800° C., 700° C., or 650°C. from the heat treatment process. The heat treatment process may beconducted in a furnace having a temperature of up to 1200° C., such asup to 1100° C., up to 1000° C., up to 900° C., up to 800° C., up to 700°C., or up to 650° C. The furnace may operate at a temperature of 700°C., such that the substrate reaches a temperature of 640° C. to burn offthe mask coating layer and/or the temporary protective layer to beremoved during the heat treatment process. In some non-limitingembodiments, the burnable material may be removed during standard heattreatment processes, such as tempering, heat strengthening, or bendingor during a heat treatment specifically performed to remove the burnablematerial without adversely affecting the substrate, as previouslydescribed. In some non-limiting examples, the burnable material may beremoved during a standard tempering procedure in which the temperingovens operate in the range of 500° C.-1000° C.

The mask coating layer and/or the temporary protective layer may beconfigured to be removable by the heat treatment process withoutsubstantially damaging the first section of the substrate. As usedherein, “substantially damaging” is defined as a change that isdetrimental to the function or aesthetics of the first section of thesubstrate that constitutes any unwanted change in a substrate propertythat would make the substrate unacceptable for its intended purpose. Forexample, substantially damaging the surface may include substantialdiscoloration to the surface from the heat treatment process. In otherapplications where a heating step is part of the standard procedure, thedamage may be defined as an unwanted color change due to the presence ofthe mask coating layer and/or the temporary protective layer. As usedherein, substantial discoloration means a color change (DECMC) of morethan 3 units, more than 2 units, or more than 1 unit compared to thecolor of a similar substrate processed without the mask coating layerand/or the temporary protective layer. DECMC (CIELAB) may be measuredusing an integrating sphere with D65 Illumination, 10° observer withspecular component included according to ASTM Designation: D 2244 - 05unless otherwise stated. Other examples of substantial damage include orcould be induced by a change in surface roughness, a change in theoxidation state of the surface, or a change in surface energy due to thepresence of the mask coating layer and/or the temporary protective layerduring the heat treatment process, or an unwanted reaction between themask coating layer and/or the temporary protective layer and thesubstrate during the heat treatment process. Substantial damage mayinclude any detrimental change to the functional coating layer (e.g., ananti-microbial functional coating that no longer sanitizes the surfaceafter the heat treatment process, a hydrophobic functional coating thatloses its hydrophobicity after the heat treatment process, a colorchange to the functional coating discernable by the human eye (e.g.,DECMC>3, 2, or 1) compared to a substrate heated without the maskcoating layer and/or the temporary protective layer.

Referring to FIG. 4 , a plan view of a segmented substrate 401 is shownaccording to some non-limiting embodiments. The segmented substrate 401may include the first section 404 of the substrate exposed with thecoating layer 410 positioned over the second section of the substrate410, but not over the first section 404 of the substrate. The coatinglayer 410 may be exposed as an outermost layer of the segmentedsubstrate 401. The segmented substrate may be prepared by providing anyof the previously-described substrates having a burnable coating maskand applying a heat treatment to the substrate having the burnablecoating mask such that the mask coating layer is removed from the firstsection 404 and thereby any coating that is applied over the maskcoating layer is also removed. The heat treatment may also remove any ofthe previously-described temporary protective layers.

A method of segmenting a substrate having at least one layer thereovermay include providing any of the previously-described substrates havinga burnable coating mask and heating the substrate having the burnablecoating mask such that the mask coating layer and the portion of thefunctional coating over the mask coating layer are removed from thefirst section. The heating step may also remove any of thepreviously-described temporary protective layers. The heating step mayincluding any of the previously-described heat treatment processes.

A method of preparing a segmented substrate having at least one layerthereover may include providing a substrate having a first surface and asecond surface opposite the first surface. The first surface has a firstsection and a second section adjacent the first section. A firstmaterial may be applied over the first section to form the mask coatinglayer. The mask coating layer is not applied over the second section. Afunctional material may be applied over at least a portion of the maskcoating layer and over the second section of the first surface to formthe functional coating layer of the coating layer. The substratecomprising the mask coating layer may be washed and/or shipped to adesired destination before application of the functional coating. Asecond material may be applied over at least a portion of the coatinglayer to form a temporary protective layer. The first material and thesecond material may be the same materials, or they may be different fromone another.

Referring to FIGS. 5A-5B, a transparency 514 (e.g., an automotivetransparency) is shown according to some non-limiting embodiments. Thetransparency 514 may include a first ply 516 with a first major surface518 (No. 1 surface) and an opposed second major surface 520 (No. 2surface). In the illustrated non-limiting embodiments, the first majorsurface 518 faces outside (e.g., the sun), i.e., is an outer majorsurface, and the second major surface 520 faces inside. The transparency514 may also include a second ply 522 having an outer (closer to theoutside) first major surface 524 (No. 3 surface) and an inner (second)major surface (No. 4 surface). This numbering of ply surfaces is inkeeping with conventional practice in the automotive art. The first ply516 and the second ply 522 can be bonded together in any suitablemanner, and may include a conventional interlayer 530 between the firstply 516 and the second ply 522. As shown in FIGS. 5A-5B, the first ply516 or the second ply 522 may be the segmented substrate 501 preparedfrom a substrate having a burnable coating mask. The coating layer 510may be formed over at least a portion of one of the plies 516, 522(e.g., the second section 506 thereof), such as, but not limited to,over at least a portion of the No. 3 surface 526 (FIG. 5A) or at least aportion of the No. 2 surface 520 (FIG. 5B). The functional coating 510could also be on the No. 1 surface or the No. 4 surface, if desired.After the heating and bending step described herein, the burnablecoating mask is burned away from the ply 516, 522 causing the firstsection of the ply 516, 522 to be void of any coating while the secondsection retains the coating 510.

The transparency 514 may be prepared by providing a substrate having aburnable coating mask (as the first ply 516 and/or the second ply 522)and applying a heat treatment to the substrate such that the maskcoating layer is removed from the first section 504. The substratehaving a burnable coating mask may include the temporary protectivelayer, which may be removed by the heat treatment.

The transparency 514 may be a transparency in any desired field, such asbut not limited to, transparencies for land, air, space, above water andunderwater vehicles. Additionally, while a typical “transparency” canhave sufficient visible light transmission such that materials can beviewed through the transparency, in the practice of the invention, the“transparency” need not be transparent to visible light but may betranslucent or opaque.

In some non-limiting examples, the transparency 514 may be a windshieldof a vehicle. The vehicle may utilize autonomous vehicle technology,such as a detector and/or a sensors (hereinafter referred tocollectively as a “sensor”) (e.g., infrared cameras, LIDAR, raindetectors, and the like). The sensors may be positioned inside of thevehicle, and the radiation or other sensing mechanism emitted by thesensor may travel through the transparency 514 to the outside of thevehicle to sense the surroundings. As the functional coating layer ofthe coating layer 510 of the transparency 514 may obstruct the radiationemitted by the sensor, the sensor may be positioned such that theradiation emitted therefrom travels through the first section 504 of thesegmented substrate 501. The first section 504 of the segmentedsubstrate 501 may be uncoated or have a coating thereover which does notaffect the sensing capabilities of the sensor. Therefore, the firstsection 504 may be selectively positioned on the segmented substrate 501based on the position of the sensors in the vehicle. This means that thesegmented substrate 501 may be prepared from a substrate having aburnable coating mask over the first section 504, such that thesegmented substrate 501 is compatible with the position of the sensor inthe vehicle (will not adversely affect the sensor) after the heattreatment process to remove the burnable coating mask.

In some non-limiting embodiments, method of preparing an automotivetransparency may include providing a first ply having an outer firstmajor surface and an opposing inner second major surface and providing asecond ply having a burnable coating mask as previously described.Alternatively, the first ply may have the burnable coating mask aspreviously described. The second ply has an inner third major surfaceand an opposing outer fourth major surface, the third major surfacehaving a first section and a second section adjacent the first section.The mask coating layer may be over the first section. The functionalcoating layer may be over at least a portion of the mask coating layerand over the second section.

The method may include heating the first ply and the second ply to atemperature sufficient to bend the first ply and the second ply. Heatingthe first ply or the second ply may include heating the first ply or thesecond ply to a temperature such that the mask coating layer is removedfrom the first section. The temperature may be at most 1000° C.

Bending the first ply and the second ply may include bending the firstply and the second ply together. Bending the first ply and the secondply may include bending the first ply and the second ply separately.Bending the plies may occur during heating. The bent first ply and bentsecond ply may be joined to one another to form an automotivetransparency in any way that two plies are typically joined to formautomotive transparencies.

An interlayer may be positioned between the first ply and the secondply, or the first bent ply and the second bent ply prior to adhering thefirst bent ply and the second bent ply, or after the first ply is heatedand bent, or after the second ply is heated and bent, or after the firstply and the second ply is heated and bent. The interlayer can be of anydesired material and can include one or more layers or plies. Theinterlayer can be a polymeric or plastic material, such as, for example,polyvinylbutyral, plasticized polyvinyl chloride, or multi-layeredthermoplastic materials including polyethyleneterephthalate, and thelike. Suitable interlayer materials are disclosed, for example, in U.S.Pat. Nos. 4,287,107 and 3,762,988. The interlayer may secure the firstand second plies together, and can provide energy absorption, reducenoise, and increase the strength of the laminated structure.Alternatively, the first and second plies can be joined together throughother means. The interlayer can also be a sound-absorbing or attenuatingmaterial as described, for example, in U.S. Pat. No. 5,796,055. Theinterlayer can have a functional coating layer provided thereon orincorporated therein or can include a colored material to reduce solarenergy transmission and/or to provide a color to the transparency. Inone non-limiting embodiment, the interlayer may be polyvinylbutyral andhave a thickness in the range of 0.5 mm to 1.5 mm, such as 0.75 mm to0.8 mm (See FIG. 5 ).

The present invention further includes the subject matter of thefollowing clauses.

Clause 1: A substrate having a burnable coating mask, comprising: asubstrate having a first surface and a second surface opposite the firstsurface; the first surfacing having a first section and a second sectionadjacent the first section; a mask coating layer over the first section,wherein the mask coating layer is not positioned over the secondsection; and a functional coating layer over at least a portion of themask coating layer and over the second section.

Clause 2: The substrate of clause 1, further comprising: a temporaryprotective layer over at least a portion of the functional coatinglayer.

Clause 3: The substrate of clause 1 or 2, wherein the substratecomprises a glass sheet.

Clause 4: The substrate of any of clauses 1-3, wherein the mask coatinglayer is in direct contact with the substrate.

Clause 5: The substrate of any of clauses 1-4, wherein the mask coatinglayer comprises at least one of a wax, an organic oil, a (meth)acrylate,a polyolefin, a polyester, a polycarbonate, a polyether, a polyurethanematerial, an epoxide material, a polyurea material, or some combinationthereof.

Clause 6: The substrate of clause 5, wherein the mask coating layercomprises at least one of polylactic acid (PLA), polyethylene carbonate(PEC), polypropylene carbonate (PPC), polycaprolactone,polyoxymethylene, polyethylene, polypropylene, an aqueous polyurethane,a polyurethane formed from a two component system, an epoxy functionalpolymeric material, or some combination thereof.

Clause 7: The substrate of any of clauses 2-6, wherein the temporaryprotective layer comprises at least one of a wax, an organic oil, a(meth)acrylate, a polyolefin, a polyester, a polycarbonate, a polyether,or some combination thereof.

Clause 8: The substrate of any of clauses 1-7, wherein the mask coatinglayer further comprises additional components including plasticizers,crosslinkers, viscosity modifiers, corrosion inhibitors, infrared (IR)absorbers, adhesion modifiers, UV absorbers, pigments, surfactants,hydrophobic agents, or a combination thereof.

Clause 9: The substrate of any of clauses 1-8, wherein the mask coatinglayer is removable by burning at a temperature of at most 1000° C.

Clause 10: The substrate of any of clauses 1-9, wherein the mask coatinglayer is configured to be removable by a heat treatment process withoutsubstantial damage to the first section.

Clause 11: The substrate of any of the clauses 1-10 further comprising aprotective layer positioned over at least a portion of the functionalcoating layer.

Clause 12: The substrate of clause 11 wherein the protective layer isselected from the group consisting of a metal oxide or a metal nitride.

Clause 13: A method of segmenting a substrate having a layer thereover,comprising: providing a substrate having a burnable coating mask,comprising: a substrate having a first surface and a second surfaceopposite the first surface; the first surface having a first section anda second section adjacent the first section; a mask coating layer overthe first section, wherein the mask coating layer is not positioned overthe second section; and a functional coating layer over at least aportion of the mask coating layer and over the second section; andheating the substrate having the burnable coating mask such that themask coating layer and a portion of the functional coating layerpositioned over the mask coating layer are removed from the firstsection.

Clause 14: The method of clause 13, wherein the substrate having theburnable coating mask further comprises a temporary protective layerover at least a portion of the functional coating layer, wherein theheat treatment removes the temporary protective layer from thefunctional coating layer.

Clause 15: The method of clause 13 or 14, wherein the substratecomprises a glass sheet.

Clause 16: The method of any of clauses 13-15, wherein the mask coatinglayer is in direct contact with the substrate.

Clause 17: The method of any of clauses 13-16, wherein the mask coatinglayer comprises at least one of a wax, an organic oil, a (meth)acrylate,a polyolefin, a polyester, a polycarbonate, a polyether, a polyurethanematerial, an epoxide material, a polyurea material, or some combinationthereof.

Clause 18: The method of clause 17, wherein the mask coating layercomprises at least one of polylactic acid (PLA), polyethylene carbonate(PEC), polypropylene carbonate (PPC), polycaprolactone,polyoxymethylene, polyethylene, polypropylene, an aqueous polyurethane,a polyurethane formed from a two component system, an epoxy functionalpolymeric material, or some combination thereof.

Clause 19: The method of any of clauses 14-18, wherein the temporaryprotective layer comprises at least one of a wax, an organic oil, a(meth)acrylate, a polyolefin, a polyester, a polycarbonate, a polyether,or some combination thereof.

Clause 20: The method of any of clauses 13-19, wherein the mask coatinglayer further comprises additional components including plasticizers,crosslinkers, viscosity modifiers, corrosion inhibitors, infrared (IR)absorbers, adhesion modifiers, UV absorbers, pigments, surfactants,hydrophobic agents, or a combination thereof.

Clause 21: The method of any of clauses 13-20, wherein the heating stepcomprises heating the substrate having the burnable coating mask at atemperature of at most 1000° C.

Clause 22: The method of any of the clauses 13-21 further comprising aprotective layer positioned over at least a portion of the functionalcoating layer.

Clause 23: The method of clause 22 wherein the protective layer isselected from the group consisting of a metal oxide or a metal nitride.

Clause 24: The method of any of clauses 13-23, wherein the mask coatinglayer is configured to be removable by the heat treatment withoutsubstantial damage to the first section.

Clause 25: A method of preparing a segmented substrate having a layerthereover, comprising: providing a substrate having a first surface anda second surface opposite the first surface; the first surface having afirst section and a second section adjacent the first section; applyinga material over the first section to form a mask coating layer, whereinthe mask coating layer is not applied over the second section; andapplying a functional material over at least a portion of the maskcoating layer and over the second section to form a functional coatinglayer.

Clause 26: The method of clause 25, further comprising: applying asecond material over at least a portion of the functional coating layerto form a temporary protective layer.

Clause 27: The method of clause 25 or 26, wherein the substratecomprises a glass sheet.

Clause 28: The method of any of clauses 25-27, wherein the mask coatinglayer is in direct contact with the substrate.

Clause 29: The method of any of clauses 25-28, wherein the mask coatinglayer comprises at least one of a wax, an organic oil, a (meth)acrylate,a polyolefin, a polyester, a polycarbonate, a polyether, a polyurethanematerial, an epoxide material, a polyurea material, or some combinationthereof.

Clause 30: The method of clause 29, wherein the mask coating layercomprises at least one of polylactic acid (PLA), polyethylene carbonate(PEC), polypropylene carbonate (PPC), polycaprolactone,polyoxymethylene, polyethylene, polypropylene, an aqueous polyurethane,a polyurethane formed from a two component system, an epoxy functionalpolymeric material, or some combination thereof.

Clause 31: The method of any of clauses 26-30, wherein the temporaryprotective layer comprises at least one of a wax, an organic oil, a(meth)acrylate, a polyolefin, a polyester, a polycarbonate, a polyether,or some combination thereof.

Clause 32: The method of any of clauses 25-31, wherein the mask coatinglayer further comprises additional components including plasticizers,crosslinkers, viscosity modifiers, corrosion inhibitors, infrared (IR)absorbers, adhesion modifiers, UV absorbers, pigments, surfactants,hydrophobic agents, or a combination thereof.

Clause 33: The method of any of clauses 25-32, further comprising:applying a heat treatment to the substrate having the burnable coatingmask at a temperature of at most 1000° C.

Clause 34: The method of any of clauses 25-33, wherein the mask coatinglayer is configured to be removable by a heat treatment withoutsubstantial damage to the first section.

Clause 35: The method of any of clauses 25-34 further comprising aprotective layer positioned over at least a portion of the functionalcoating layer.

Clause 36: The method of clause 35 wherein the protective layer isselected from the group consisting of silicon nitride, Si₃N₄, SiAlN,SiAlON, titania, alumina, silica, zirconia, tin oxide, a mixturethereof, and an alloy thereof.

Clause 37: The method of any of the clauses 25-36 wherein the secondmaterial is different than the material.

Clause 38: The method of any of the clauses 25-36 wherein the secondmaterial is the same as the material.

Clause 39: A segmented substrate prepared by: providing a substratehaving a burnable coating mask, comprising: a substrate having firstsurface and a second surface opposite the first surface; the firstsurface having a first section and a second section adjacent the firstsection; a mask coating layer over the first section, wherein the maskcoating layer is not positioned over the second section; and afunctional coating layer over at least a portion of the mask coatinglayer and over the second section; heating the substrate having theburnable coating mask such that the mask coating layer and a portion ofthe functional coating that is positioned over the mask coating layerare removed from the first section.

Clause 40: The segmented substrate of clause 41, wherein the substratehaving the burnable coating mask further comprises a temporaryprotective layer over at least a portion of the functional coatinglayer, wherein the heat treatment removes the temporary protectivelayer.

Clause 41: The segmented substrate of clause 39 or 40, wherein thesubstrate comprises a glass sheet.

Clause 42: The segmented substrate of any of clauses 39-41, wherein themask coating layer is in direct contact with the substrate.

Clause 43: The segmented substrate of any of clauses 39-42, wherein themask coating layer comprises at least one of a wax, an organic oil, a(meth)acrylate, a polyolefin, a polyester, a polycarbonate, a polyether,a polyurethane material, an epoxide material, a polyurea material, orsome combination thereof.

Clause 44: The segmented substrate of clause 43, wherein the maskcoating layer comprises at least one of polylactic acid (PLA),polyethylene carbonate (PEC), polypropylene carbonate (PPC),polycaprolactone, polyoxymethylene, polyethylene, polypropylene, anaqueous polyurethane, a polyurethane formed from a two component system,an epoxy functional polymeric material, or some combination thereof.

Clause 45: The segmented substrate of any of clauses 40-44, wherein thetemporary protective layer comprises at least one of a wax, an organicoil, a (meth)acrylate, a polyolefin, a polyester, a polycarbonate, apolyether, or some combination thereof.

Clause 46: The segmented substrate of any of clauses 39-45, wherein themask coating layer further comprises additional components includingplasticizers, crosslinkers, viscosity modifiers, corrosion inhibitors,infrared (IR) absorbers, adhesion modifiers, UV absorbers, pigments,surfactants, hydrophobic agents, or a combination thereof.

Clause 47: The segmented substrate of any of clauses 39-46, wherein theheat treatment comprises heating the substrate having the burnablecoating mask at a temperature of at most 1000° C.

Clause 48: The segmented substrate of any of clauses 39-47, wherein themask coating layer is configured to be removable by the heat treatmentwithout substantial damage to the first section.

Clause 49: The segmented substrate of any of the clauses 39-48 furthercomprising a protective layer positioned over at least a portion of thefunctional coating layer.

Clause 50: The method of clause 49 wherein the protective layer isselected from the group consisting of silicon nitride, Si₃N₄, SiAlN,SiAlON, titania, alumina, silica, zirconia, tin oxide, a mixturethereof, and an alloy thereof.

Clause 51: A method of preparing an automotive transparency, comprising:providing a first ply having a No. 1 surface and a No. 2 surfaceopposite the No. 1 surface; providing a second ply having a No. 3surface and a No. 4 surface opposite the No. 3 surface; applying aburnable coating mask to a first section of the No. 1 surface, No. 2,surface, No. 3 surface or No. 4 surface, wherein the burnable coatingmask is not applied to a second section of the No. 1 surface, No. 2,surface, No. 3 surface or No. 4 surface; and applying a functionalcoating layer over at least a portion of the mask coating layer and overthe second section; heating the first ply and the second ply eithersimultaneously or separately; and joining the first ply and the secondply to one another to form the automotive transparency.

Clause 52: The method of clause 51, further comprising: bending thefirst ply and bending the second ply either simultaneously orseparately.

Clause 53: The method of clause 51 or 52, wherein the first ply and thesecond ply are heated separately.

Clause 54: The method of clause 52 or 53, wherein the first ply and thesecond player are bent separately.

Clause 55: The method of any of the clauses clause 51-54, furthercomprising: positioning an interlayer between the first ply and thesecond ply.

Clause 56: The method of any of clauses 51-55, wherein heating thesecond ply comprises heating the second ply to a temperature such thatthe mask coating layer and a portion of the functional coatingpositioned over the mask coating layer are removed from the firstsection.

Clause 57: The method of clause 56, wherein the temperature is at most1000° C.

Clause 58: A method of preparing an automotive transparency, comprising:providing a ply having a first major surface and a second major surfaceopposite the first major surface, wherein the first major surfacecomprises a first section and a second section adjacent the firstsection, wherein a mask coating layer is positioned over the firstsection, wherein the mask coating layer is not positioned over thesecond section; and wherein a functional coating layer is positionedover a portion of the mask coating layer and over the second section;heating the ply whereby the mask coating layer and a portion of thefunctional coating layer positioned over the mask coating layer areremoved from the first section; and bending the ply.

Clause 59: The method of clause 58, wherein the temperature is at most1000° C.

The following example is presented to demonstrate the general principlesof the invention of this disclosure. The invention should not beconsidered as limiting to the specific example presented.

EXAMPLE

A coated substrate comprising a mask coating layer was preparedaccording to the following procedure. A 12″x12″ and 6 mm thick clearglass substrate was provided. The glass substrate was washed in anindustry washer. An epoxy acrylate UV curable resin was diluted withacetone until a 50:50 ratio of components was achieved. A small area ofthe diluted epoxy acrylate UV curable resin was added to the surface ofthe glass substrate using an eyedropper. The small area of diluted epoxyacrylate UV curable resin was left to dry and then was subsequentlycured using ultraviolet light with an energy density of 250-300 mJ/cm²to produce a mask coating layer. The thickness of the mask coating layerwas in the range of 7-10 µm. The glass substrate with mask coating layerwas then washed again in an industry washer. After washing, the glasssubstrate with mask coating layer was placed in a pilot coater and aSolarban® 60VT double silver functional coating was deposited over theglass substrate and the mask coating layer to produce a coatedsubstrate. The coated substrate was then placed in a box furnace set toa temperature of 700° C. (1292° F.). The coated substrate was heated inthe box furnace until a glass temperature of about 1,180° F.(approximately 640° C.) was reached. The coated substrate was thenremoved from the box furnace and left to cool to room temperature (i.e.,between 20-30° C.). FIG. 6 is a micrograph of the coated substrate takenafter the coated substrate was removed from the box furnace and allowedto cool to room temperature. As shown in FIG. 6 , the area that includedthe mask coating layer under the functional coating (i.e., bottom andleft regions) was removed during heating in the box furnace. Outside ofthe area including the mask coating layer (i.e., top and right regions),the functional coating remained intact. At the boundary between the areaof the coated substrate that included the mask coating layer and thearea that did not include the mask coating layer, a small amount ofdebris can been seen. The coated substrate was washed in an industrywasher to remove the remaining debris of the mask coating layer and/orfunctional coating that remained after heating. Thus, this Exampleeffectively demonstrates the ability of the present invention to producea coated substrate comprising a functional coating over a first regionof the substrate and no functional coating over a second region of thesubstrate.

Although the invention has been described in detail for the purpose ofillustration based on what is currently considered to be the mostpractical and preferred embodiments, it is to be understood that suchdetail is solely for that purpose and that the invention is not limitedto the disclosed embodiments, but, on the contrary, is intended to covermodifications and equivalent arrangements that are within the spirit andscope of the appended claims. For example, it is to be understood thatthe present invention contemplates that, to the extent possible, one ormore features of any embodiment can be combined with one or morefeatures of any other embodiment.

The invention claimed is:
 1. A segmented substrate prepared by a processcomprising the steps of: providing a substrate having a burnable coatingmask, the substrate comprising: a substrate having a first surface and asecond surface opposite the first surface, the first surface having afirst section and a second section adjacent the first section; a maskcoating layer over the first section, wherein the mask coating layer isnot positioned over the second section; and a functional coating layerover at least a portion of the mask coating layer and over the secondsection; heating the substrate having the burnable coating mask suchthat the mask coating layer and a portion of the functional coating thatis positioned over the mask coating layer are removed from the firstsection.
 2. The segmented substrate of claim 1, wherein the substratehaving the burnable coating mask further comprises a temporaryprotective layer over at least a portion of the functional coatinglayer, and wherein the heat treatment removes the temporary protectivelayer.
 3. The segmented substrate of claim 1, wherein the substratecomprises a glass sheet.
 4. The segmented substrate of claim 1, whereinthe mask coating layer is in direct contact with the substrate.
 5. Thesegmented substrate of claim 1, wherein the mask coating layer comprisesat least one of a wax, an organic oil, a (meth)acrylate, a polyolefin, apolyester, a polycarbonate, a polyether, a polyurethane material, anepoxide material, a polyurea material, or some combination thereof. 6.The segmented substrate of claim 1, wherein the mask coating layercomprises at least one of polylactic acid (PLA), polyethylene carbonate(PEC), polypropylene carbonate (PPC), polycaprolactone,polyoxymethylene, polyethylene, polypropylene, an aqueous polyurethane,a polyurethane formed from a two component system, an epoxy functionalpolymeric material, or some combination thereof.
 7. The segmentedsubstrate of claim 2, wherein the temporary protective layer comprisesat least one of a wax, an organic oil, a (meth)acrylate, a polyolefin, apolyester, a polycarbonate, a polyether, or some combination thereof. 8.The segmented substrate of claim 1, wherein the mask coating layerfurther comprises additional components including plasticizers,crosslinkers, viscosity modifiers, corrosion inhibitors, infrared (IR)absorbers, adhesion modifiers, UV absorbers, pigments, surfactants,hydrophobic agents, or a combination thereof.
 9. The segmented substrateof claim 1, wherein the heat treatment comprises heating the substratehaving the burnable coating mask at a temperature of at most 1000° C.10. The segmented substrate of claim 1, wherein the mask coating layeris configured to be removable by the heat treatment without substantialdamage to the first section.
 11. The segmented substrate of claim 1,further comprising a protective layer positioned over at least a portionof the functional coating layer.
 12. The segmented substrate of claim11, wherein the protective layer is selected from the group consistingof silicon nitride, Si3N4, SiAlN, SiAlON, titania, alumina, silica,zirconia, tin oxide, a mixture thereof, and an alloy thereof.
 13. Atransparency comprising: a first ply having a number one surface and anumber two surface opposite the number one surface; a second ply havinga number three surface and a number four surface opposite the numberthree surface; and at least one interlayer located between the numbertwo surface and the number three surface, the interlayer designed tobond the first ply to the second ply, wherein at least one of the firstply or the second ply is a segmented substrate formed from a substratehaving a burnable coating mask comprising: a substrate having a firstsurface and a second surface opposite the first surface, wherein thefirst surface of the substrate comprises a first section and a secondsection adjacent the first section; a burnable mask coating layer overthe first section, wherein the burnable mask coating layer is notpresent over the second section; and a functional coating layer over atleast a portion of the mask coating layer and over the second section,wherein the burnable mask coating layer is removed via a heat treatmentsuch that the mask coating layer is removed from the first section, afirst portion of the functional coating positioned over at least theportion of the mask coating layer is removed, and a second portion ofthe functional coating layer that is positioned over the second sectionremains on the substrate to yield the segmented substrate that forms oneof at least the first ply or the second ply.
 14. The transparency ofclaim 13, wherein the mask coating layer comprises at least one of awax, an organic oil, a (meth)acrylate, a polyolefin, a polyester, apolycarbonate, a polyether, a polyurethane material, an epoxidematerial, a polyurea material, or some combination thereof.
 15. Thetransparency of claim 13, wherein the mask coating layer comprises atleast one of polylactic acid (PLA), polyethylene carbonate (PEC),polypropylene carbonate (PPC), polycaprolactone, polyoxymethylene,polyethylene, polypropylene, an aqueous polyurethane, a polyurethaneformed from a two component system, an epoxy functional polymericmaterial, or some combination thereof.
 16. The transparency of claim 13,wherein the mask coating layer is removable by burning at a temperatureof at most 1000° C.
 17. A substrate having a burnable coating maskcomprising: a substrate having a first surface and a second surfaceopposite the first surface, the first surface comprising a first sectionand a second section adjacent the first section; a mask coating layerover the first section, wherein the mask coating layer is not presentover the second section; and a functional coating layer over at least aportion of the mask coating layer and over the second section, whereinthe mask coating layer comprises at least one of a wax, an organic oil,a polyolefin, a polyester, a polycarbonate, a polyether, an aqueouspolyurethane, a polyurethane formed from a two component system, apolyurea material, a polylactic acid (PLA), a polyethylene carbonate(PEC), a polypropylene carbonate (PPC), a polycaprolactone, apolyoxymethylene, a polyethylene, a polypropylene, an aqueouspolyurethane, a polyurethane formed from a two component system, or somecombination thereof.